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Article Publish Status: FREE
Abstract Title:

Curcumol Alleviates the Inflammation of Nucleus Pulposus Cells via the PI3K/Akt/NF-κB Signaling Pathway and Delays Intervertebral Disc Degeneration.

Abstract Source:

World Neurosurg. 2021 Aug 24. Epub 2021 Aug 24. PMID: 34450323

Abstract Author(s):

Shenghua He, Yuanfei Fu, Bona Yan, Huangsheng Tan, Haokang Li, Jin Li, Dan Huang, Zhuohan Huang, Juyi Lai, Hualong Feng, Zhitao Sun, Zhiming Lan

Article Affiliation:

Shenghua He

Abstract:

BACKGROUND: Intervertebral disc degeneration (IVDD) is closely associated with inflammatory environments. Curcumol has been shown to alleviate inflammation in various disease models, but its effects on IVDD remain unclear. In this study, we sought to determine the mechanism of curcumol in TNF-α-induced nucleus pulposus cells (NPCs) and a mouse IVDD model.

METHODS: NPCs were pretreated with curcumol and then exposed to TNF-α. Cell viability was analyzed using the CCK-8, and the mRNA and protein levels of inflammatory cytokines and PI3K/Akt/NF-κB-related signaling molecules were detected using RT-PCR, ELISA and western blotting. The mouse IVDD model was established by puncturing the C6/7 level of the caudal spine, and treated with curcumol after surgery. ABOG staining were performed to evaluate the severity intervertebral disc damage, and immunohistochemistry(IHC) was performed to detect the expression of TNF-α. The toxicological effects of curcumol were measured by performing HE staining and ELISA.

RESULTS: Curcumol reduced IL-1β, IL-6 and TNF-α production in NPCs, and the phosphorylation of proteins in the PI3K/Akt/NF-κB signaling pathway was also decreased. The PI3K/Akt/NF-κB -related signaling molecules decreased when TNF-α-induced NPCs were treated with a PI3K inhibitor; however, curcumol did not reverse these effects. In vivo, curcumol ameliorated the progression of IVDD at the early stage and did not exert toxicological effects.

CONCLUSION: These results suggest a potential therapeutic use of curcumol to alleviate inflammation via the PI3K/Akt/NF-κB signaling pathway and delay the progression of IVDD.

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